AU2003282510A1 - Hexahydro-benzimidazolone compounds useful as anti-inflammatory agents - Google Patents
Hexahydro-benzimidazolone compounds useful as anti-inflammatory agentsInfo
- Publication number
- AU2003282510A1 AU2003282510A1 AU2003282510A AU2003282510A AU2003282510A1 AU 2003282510 A1 AU2003282510 A1 AU 2003282510A1 AU 2003282510 A AU2003282510 A AU 2003282510A AU 2003282510 A AU2003282510 A AU 2003282510A AU 2003282510 A1 AU2003282510 A1 AU 2003282510A1
- Authority
- AU
- Australia
- Prior art keywords
- hexahydro
- inflammatory agents
- compounds useful
- benzimidazolone compounds
- benzimidazolone
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- HMTUMIONOVAMED-UHFFFAOYSA-N 1,3,3a,4,5,6-hexahydrobenzimidazol-2-one Chemical class C1CCC=C2NC(=O)NC21 HMTUMIONOVAMED-UHFFFAOYSA-N 0.000 title 1
- 229940121363 anti-inflammatory agent Drugs 0.000 title 1
- 239000002260 anti-inflammatory agent Substances 0.000 title 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
- C07D235/26—Oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US41793502P | 2002-10-11 | 2002-10-11 | |
| US60/417,935 | 2002-10-11 | ||
| PCT/US2003/031960 WO2004032861A2 (fr) | 2002-10-11 | 2003-10-09 | Composes hexahydro-benzimidazolones utiles en tant qu'agents anti-inflammatoires |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2003282510A1 true AU2003282510A1 (en) | 2004-05-04 |
| AU2003282510A8 AU2003282510A8 (en) | 2004-05-04 |
Family
ID=32094123
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2003282510A Abandoned AU2003282510A1 (en) | 2002-10-11 | 2003-10-09 | Hexahydro-benzimidazolone compounds useful as anti-inflammatory agents |
Country Status (3)
| Country | Link |
|---|---|
| US (1) | US6974815B2 (fr) |
| AU (1) | AU2003282510A1 (fr) |
| WO (1) | WO2004032861A2 (fr) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7550590B2 (en) | 2003-03-25 | 2009-06-23 | Takeda Pharmaceutical Company Limited | Dipeptidyl peptidase inhibitors |
| EP1625122A1 (fr) | 2003-05-14 | 2006-02-15 | Takeda San Diego, Inc. | Inhibiteurs de dipeptidyl peptidase |
| US20050070531A1 (en) | 2003-08-13 | 2005-03-31 | Syrrx, Inc. | Dipeptidyl peptidase inhibitors |
| US20070060530A1 (en) | 2005-09-14 | 2007-03-15 | Christopher Ronald J | Administration of dipeptidyl peptidase inhibitors |
| EP1924567B1 (fr) | 2005-09-16 | 2012-08-22 | Takeda Pharmaceutical Company Limited | Inhibiteurs de dipeptidylpeptidase |
| US8324383B2 (en) | 2006-09-13 | 2012-12-04 | Takeda Pharmaceutical Company Limited | Methods of making polymorphs of benzoate salt of 2-[[6-[(3R)-3-amino-1-piperidinyl]-3,4-dihydro-3-methyl-2,4-dioxo-1(2H)-pyrimidinyl]methyl]-benzonitrile |
| TW200838536A (en) | 2006-11-29 | 2008-10-01 | Takeda Pharmaceutical | Polymorphs of succinate salt of 2-[6-(3-amino-piperidin-1-yl)-3-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-ylmethy]-4-fluor-benzonitrile and methods of use therefor |
| WO2008105803A1 (fr) * | 2007-02-26 | 2008-09-04 | Larry Schlesinger | Formulations topiques contenant un antagoniste du récepteur de leucotriène et utilisations associées |
| US8093236B2 (en) | 2007-03-13 | 2012-01-10 | Takeda Pharmaceuticals Company Limited | Weekly administration of dipeptidyl peptidase inhibitors |
| US8481750B2 (en) | 2009-06-02 | 2013-07-09 | Boehringer Ingelheim International Gmbh | Derivatives of 6,7-dihydro-5H-imidazo[1,2-α]imidazole-3-carboxylic acid amides |
| ES3041181T3 (en) | 2015-12-23 | 2025-11-07 | Univ Sorbonne | Agents that inhibit the binding of cfh to cd11b/cd18 and uses thereof |
Family Cites Families (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3930005A (en) * | 1973-06-15 | 1975-12-30 | Squibb & Sons Inc | Antiinflammatory agents and their use |
| EP0178413A1 (fr) * | 1984-08-17 | 1986-04-23 | Beecham Group Plc | Benzimidazoles |
| US4812462A (en) * | 1986-04-01 | 1989-03-14 | Warner-Lambert Company | 4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine-6-carboxylic acid analogs having antihypertensive activity |
| FR2597478B1 (fr) * | 1986-04-21 | 1988-12-16 | Esteve Labor Dr | Benzimidazoles et imidazopyridines sulfonamides, leur preparation et leur application en tant que medicaments. |
| DE3728695A1 (de) * | 1987-08-25 | 1989-03-09 | Schering Ag | Neue benzimidazol-derivate |
| GB8817651D0 (en) * | 1988-07-25 | 1988-09-01 | Smith Kline French Lab | Chemical compounds |
| US5128359A (en) * | 1990-02-16 | 1992-07-07 | Laboratoires Upsa | Benzimidazole and azabenzimidazole derivatives which are thromboxane receptor antagonists, their methods of preparation |
| FR2658511B1 (fr) * | 1990-02-16 | 1992-06-19 | Union Pharma Scient Appl | Nouveaux derives de benzimidazole et d'azabenzimidazole, antagonistes des recepteurs au thromboxane; leurs procedes de preparation, compositions pharmaceutiques les contenant. |
| FR2665161B1 (fr) * | 1990-07-26 | 1992-11-27 | Esteve Labor Dr | Nouveaux derives de benzimidazole, leur preparation et leur application en tant que medicaments. |
| US5817661A (en) * | 1991-12-06 | 1998-10-06 | Hoechst Marion Roussel, Inc. | Trans cyclopentanyl purine analogs useful as immunosuppressants |
| CA2134009C (fr) * | 1993-11-11 | 2005-03-08 | Oleg Werbitzky | Amidines bicycliques, methode pour leur obtention et leur utilisation comme catalyseur |
| US5716594A (en) * | 1994-06-06 | 1998-02-10 | The Jmde Trust | Biotin compounds for targetting tumors and sites of infection |
| SK117499A3 (en) | 1997-03-03 | 2000-05-16 | Boehringer Ingelheim Pharma | Small molecules useful in the treatment of inflammatory and immune cell-mediated diseases, small molecules and pharmaceutical composition with their content |
| DE69839399T2 (de) | 1997-08-28 | 2009-05-20 | Novartis Ag | Lymphozyten funktion antigen-1 antagonisten |
| AU1083499A (en) | 1997-10-21 | 1999-05-10 | Pharmacia & Upjohn Company | Thiadiazoles amides useful as antiinflammatory agents |
| WO1999020617A1 (fr) | 1997-10-21 | 1999-04-29 | Active Biotech Ab | Urees thiadiazoles anti-inflammatoires agissant comme inhibiteurs lfa-1 et mac-1 |
| WO1999049856A2 (fr) | 1998-03-27 | 1999-10-07 | Genentech, Inc. | Antagonistes destines au traitement de troubles induits par le recepteur d'adhesion de cd11/cd18 |
| US6331640B1 (en) | 1998-10-13 | 2001-12-18 | Hoffmann-La Roche Inc. | Diaminopropionic acid derivatives |
| US6110922A (en) | 1998-12-29 | 2000-08-29 | Abbott Laboratories | Cell adhesion-inhibiting antiinflammatory and immune-suppressive compounds |
| CO5140104A1 (es) | 1999-02-16 | 2002-03-22 | Novartis Ag | Derivados de mevinolina y preparacion farmaceuticas que los contienen |
| UA74781C2 (en) | 1999-04-02 | 2006-02-15 | Abbott Lab | Antiinflammatory and immumosuppressive compounds inhibiting cell adhesion |
| WO2001007044A1 (fr) | 1999-07-21 | 2001-02-01 | Boehringer Ingelheim Pharmaceuticals, Inc. | Petites molecules utiles pour le traitement de maladies inflammatoires |
| US6492408B1 (en) | 1999-07-21 | 2002-12-10 | Boehringer Ingelheim Pharmaceuticals, Inc. | Small molecules useful in the treatment of inflammatory disease |
| US6365615B1 (en) | 1999-07-21 | 2002-04-02 | Boehringer Ingelheim Pharmaceuticals, Inc. | Small molecules useful in the treatment of inflammatory disease |
| US6350763B1 (en) | 1999-07-21 | 2002-02-26 | Boehringer Ingelheim Pharmaceuticals, Inc. | Small molecules useful in the treatment of inflammation disease |
| ATE396722T1 (de) | 1999-07-21 | 2008-06-15 | Boehringer Ingelheim Pharma | Kleine moleküle zur behandlung von endzündlichen erkrankungen |
| CA2388639C (fr) | 1999-10-20 | 2007-07-17 | Tanabe Seiyaku Co., Ltd. | Inhibiteurs d'adhesion cellulaire induite par alphalbeta2 |
| WO2001051508A1 (fr) | 2000-01-14 | 2001-07-19 | Science & Technology Corporation @ Unm | Peptides inhibiteurs de l'interaction lfa-1/icam-1 |
| US6515124B2 (en) | 2000-02-09 | 2003-02-04 | Hoffman-La Roche Inc. | Dehydroamino acids |
| NZ523444A (en) | 2000-06-29 | 2004-12-24 | Abbott Lab | Aryl phenylcyclopropyl sulphide derivatives and their use as cell adhesion-inhibiting anti-inflammatory and immune-suppressive agents |
| WO2002002539A1 (fr) | 2000-06-29 | 2002-01-10 | Abbott Laboratories | Derives d'aryle phenylheterocyclyle sulfures et leur utilisation en tant qu'agents immunosuppresseurs anti-inflammatoires inhibant l'adherence cellulaire |
| US7709520B2 (en) | 2000-10-06 | 2010-05-04 | The Texas A&M University System | Diindolylmethane and C-substituted diindolylmethane compositions and methods for the treatment of multiple cancers |
| GB0028367D0 (en) | 2000-11-21 | 2001-01-03 | Celltech Chiroscience Ltd | Chemical compounds |
| CZ20031380A3 (cs) | 2000-11-28 | 2003-10-15 | Genentech, Inc. | LFA-1 Antagonistické sloučeniny |
| AU2002227128A1 (en) * | 2000-12-01 | 2002-06-11 | Bristol-Myers Squibb Company | Hydantoin compounds useful as anti-inflammatory agents |
-
2003
- 2003-10-09 AU AU2003282510A patent/AU2003282510A1/en not_active Abandoned
- 2003-10-09 WO PCT/US2003/031960 patent/WO2004032861A2/fr not_active Ceased
- 2003-10-09 US US10/681,924 patent/US6974815B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| US20040116467A1 (en) | 2004-06-17 |
| WO2004032861A3 (fr) | 2004-08-05 |
| US6974815B2 (en) | 2005-12-13 |
| WO2004032861A2 (fr) | 2004-04-22 |
| AU2003282510A8 (en) | 2004-05-04 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MK6 | Application lapsed section 142(2)(f)/reg. 8.3(3) - pct applic. not entering national phase |